Canonical Allele Identifier: CA500206360
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780477C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624225C>T , CM000679.2:g.41624225C>T GRCh38
NC_000017.10:g.39780477C>T , CM000679.1:g.39780477C>T GRCh37
NC_000017.9:g.37034003C>T NCBI36
NG_008625.1:g.5406G>A
NG_009090.2:g.167488G>A , LRG_401:g.167488G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.285G>A MANE Select ENSP00000308452.8:p.Leu95=
ENST00000311208.12:c.285G>A ENSP00000308452.8:p.Leu95=
ENST00000463128.5:c.-312-19G>A ENSP00000468672.1:n.-312-19G>A
ENST00000491673.1:n.351G>A
ENST00000493253.5:n.72G>A
ENST00000540235.5:c.71+9G>A ENSP00000441751.2:n.71+9G>A
ENST00000577817.3:c.240G>A ENSP00000467418.1:p.Leu80=
NM_000422.2:c.285G>A NP_000413.1:p.Leu95=
NM_000422.3:c.285G>A MANE Select NP_000413.1:p.Leu95=